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Enantioselective Synthesis and Activity of All Diastereoisomers of ( E)-Phytal, a Pheromone Component of the Moroccan Locust, Dociostaurus maroccanus.

Publicated to:Journal Of Agricultural And Food Chemistry. 67 (1): 72-80 - 2019-01-09 67(1), doi: 10.1021/acs.jafc.8b06346

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Affiliations

CSIC, Inst Adv Chem Catalonia, Dept Biol Chem & Mol Modelling, ES-08034 Barcelona, Spain - Author
Department of Biological Chemistry and Molecular Modelling , Institute of Advanced Chemistry of Catalonia (CSIC) , 08034 Barcelona , Spain. - Author
European Regional Development FundEuropean Union (EU) - Funding
MINECOSpanish Ministry of Economy & Competitiveness [AGL2012-39869-C02-01, AGL2015-66469-R] - Funding
Plant Health Department , Centro de Investigación y Tecnología Agroalimentaria de Aragón and Instituto Agroalimentario de Aragón-IA2, CITA-Zaragoza University , 50059 Zaragoza , Spain. - Author
Regional Community of Aragon - Funding
Univ Zaragoza, Ctr Invest & Tecnol Agroalimentaria Aragon, Plant Hlth Dept, CITA, Zaragoza 50059, Spain - Author
Univ Zaragoza, Inst Agroalimentario Aragon, CITA, Zaragoza 50059, Spain - Author
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Abstract

Keywords: (2e,7r,11r)-3,7,11,15-tetramethylhexadec-2-enal; Behavioral activity; Dociostaurus maroccanus; Electrophysiology; Enantioselective synthesis; Moroccan locust; Phytal; Sex pheromone

Quality index

WoS Scopus by Scimago
Best Categ.Agriculture, MultidisciplinaryAgricultural and Biological Sciences (Miscellaneous)
WoSScopus by ScimagoSPIFecytAgaurDialnetCircCapesMiar
IF4.1921.086--11.000
Rank4/5832/228
QQ1Q1-----A1
DD1D2-
TT1T1
PP94P15
Index ERIC-
Index Emergin-
Index AHCI-